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J Jay Gargus

Showing results (11-20 of 21) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 23, 2005
Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2Laura Segall, Alessandra Mezzetti, Rosemarie Scanzano, et al.
Molecular Genetics and Metabolism Reports|October 26, 2020
Diffuse large B-cell non-Hodgkin's lymphoma in Gaucher diseaseGrant Bonesteele, J Jay Gargus, Emily Curtin, et al.
Journal of Autism and Developmental Disorders|February 1, 2005
Relative carnitine deficiency in autismPauline A Filipek, Jenifer Juranek, Minh T Nguyen, et al.
Cell Reports|January 21, 2015
Disruption of Transient Serotonin Accumulation by Non-Serotonin-Producing Neurons Impairs Cortical Map DevelopmentXiaoning Chen, Ran Ye, J Jay Gargus, et al.
Scientific Reports|February 2, 2017
High-throughput screen detects calcium signaling dysfunction in typical sporadic autism spectrum disorderGalina Schmunk, Rachel L Nguyen, David L Ferguson, et al.
The Journal of Biological Chemistry|August 17, 2004
Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2Laura Segall, Rosemarie Scanzano, Mari A Kaunisto, et al.
The Journal of Biological Chemistry|November 26, 2003
SK3-1C, a dominant-negative suppressor of SKCa and IKCa channelsAaron Kolski-Andreaco, Hiroaki Tomita, Vikram G Shakkottai, et al.
Annals of Neurology|June 5, 2003
Mitochondrial dysfunction in autistic patients with 15q inverted duplicationPauline A Filipek, Jenifer Juranek, Moyra Smith, et al.
Orphanet Journal of Rare Diseases|February 10, 2017
Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation studySimon A Jones, Sandra Rojas-Caro, Anthony G Quinn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 28, 2015
Rapid progression and mortality of lysosomal acid lipase deficiency presenting in infantsSimon A Jones, Vassili Valayannopoulos, Eugene Schneider, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|July 23, 2005
Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2Laura Segall, Alessandra Mezzetti, Rosemarie Scanzano, et al.
Molecular Genetics and Metabolism Reports|October 26, 2020
Diffuse large B-cell non-Hodgkin's lymphoma in Gaucher diseaseGrant Bonesteele, J Jay Gargus, Emily Curtin, et al.
Journal of Autism and Developmental Disorders|February 1, 2005
Relative carnitine deficiency in autismPauline A Filipek, Jenifer Juranek, Minh T Nguyen, et al.
Cell Reports|January 21, 2015
Disruption of Transient Serotonin Accumulation by Non-Serotonin-Producing Neurons Impairs Cortical Map DevelopmentXiaoning Chen, Ran Ye, J Jay Gargus, et al.
Scientific Reports|February 2, 2017
High-throughput screen detects calcium signaling dysfunction in typical sporadic autism spectrum disorderGalina Schmunk, Rachel L Nguyen, David L Ferguson, et al.
The Journal of Biological Chemistry|August 17, 2004
Kinetic alterations due to a missense mutation in the Na,K-ATPase alpha2 subunit cause familial hemiplegic migraine type 2Laura Segall, Rosemarie Scanzano, Mari A Kaunisto, et al.
The Journal of Biological Chemistry|November 26, 2003
SK3-1C, a dominant-negative suppressor of SKCa and IKCa channelsAaron Kolski-Andreaco, Hiroaki Tomita, Vikram G Shakkottai, et al.
Annals of Neurology|June 5, 2003
Mitochondrial dysfunction in autistic patients with 15q inverted duplicationPauline A Filipek, Jenifer Juranek, Moyra Smith, et al.
Orphanet Journal of Rare Diseases|February 10, 2017
Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation studySimon A Jones, Sandra Rojas-Caro, Anthony G Quinn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 28, 2015
Rapid progression and mortality of lysosomal acid lipase deficiency presenting in infantsSimon A Jones, Vassili Valayannopoulos, Eugene Schneider, et al.
Pageof 3